| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108664789-108665120 | Common:5; Rare:126 | ||||
| chr11:108929328-108929605 | Common:1; Rare:52 | ||||
| chr11:111602204-111602472 | Common:1; Rare:90 | ||||
| chr11:111766353-111766415 | Rare:34 | ||||
| chr11:111871279-111871334 | Rare:16 | ||||
| chr11:111878903-111878964 | Common:1; Rare:21 | ||||
| chr11:111879152-111879542 | Rare:118 | ||||
| chr11:111911948-111912001 | Common:1; Rare:11 | ||||
| chr11:112025301-112025475 | Common:2; Rare:39; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074415 | Common:1; Rare:85 | ||||
| chr11:112086686-112086905 | Rare:97; Clinvar:1 | ||||
| chr11:112226333-112226462 | Rare:62 | ||||
| chr11:113314393-113314602 | Rare:71 | ||||
| chr11:113875493-113875771 | Common:4; Rare:101 | ||||
| chr11:114400450-114400766 | Common:2; Rare:123 |